Colon Cancer: Gene >> CNN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000252456
Start	11538943:11538943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.16T>G
AA Mutation	p.Phe6Val(p.F6V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000252456
Start	11549612:11549612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.711C>A
AA Mutation	p.His237Gln(p.H237Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000252456
Start	11546738:11546738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.249C>A
AA Mutation	p.His83Gln(p.H83Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000252456
Start	11541178:11541178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.166G>T
AA Mutation	p.Asp56Tyr(p.D56Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000252456
Start	11549709:11549709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.808C>A
AA Mutation	p.Pro270Thr(p.P270T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000252456
Start	11549326:11549326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505G>A
AA Mutation	p.Gly169Ser(p.G169S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000252456
Start	11541142:11541142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748140771
CDS Mutation	c.130C>T
AA Mutation	p.Arg44Cys(p.R44C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252456
Start	11546888:11546888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370744850
CDS Mutation	c.309C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252456
Start	11549705:11549705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376859144
CDS Mutation	c.804C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252456
Start	11541126:11541126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.114C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000252456
Start	11546893:11546893(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.318delT
AA Mutation	p.Phe106LeufsTer33(p.F106Lfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CNN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000252456
Start	11549426:11549426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745990452
CDS Mutation	c.605C>T
AA Mutation	p.Ala202Val(p.A202V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000252456
Start	11549644:11549644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.743G>A
AA Mutation	p.Gly248Asp(p.G248D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript